- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06495099
Effect of Core Stability Exercises and Russian Electrical Stimulation in Non-specific Low Back Pain
June 24, 2025 updated by: Deraya University
Effect of Core Stability Exercises and Russian Electrical Stimulation in Non-specific Low Back Pain (Randomized Control Trail)
Brief Summary: Low back pain (LBP) is an important public health problem due to the increasing world population and aging.
In chronic LBP, exercise therapy is among the first-line treatments.
Core stabilization exercises (CSE), one of the motor control exercises, focus on the activation and control of the deep spinal muscles.
Recently, some studies have shown that Russian electrical stimulation alone or combined with exercise can provide contraction in deep stabilizer muscles and significantly reduce pain in patients with LBP
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Minya, Egypt, 05673
- Deraya university
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- The duration of the disease is more than 3 months with pain scores greater than four in the VAS disability score of 19% or greater as evident from the modified oswestry disability.
Exclusion Criteria:
- Neurological or musculoskeletal diseases that affect lumbar spine (e.g: lumbar spondylosis, spondylolisthesis, and lumbar disc injuries)
- women during pregnancy and lactation.
- History of lumbar spine surgery.
- Signs of lumbar radiculopathy or myelopathy.
- Signs of serious pathology (e.g., malignancy, inflammatory disorders, infection
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: group A
The training group A will be treated by core stability exercises and Russian electrical stimulation
|
Type of Medium frequency current with 2500 Hz frequency modulated at 50 Hz with 50% Duty cycle training protocol is (10 sec.
on time - 50 sec.
off time - 10 minutes total time)
|
|
Active Comparator: group B
The training group B will be treated by core stability exercises.
|
Type of Medium frequency current with 2500 Hz frequency modulated at 50 Hz with 50% Duty cycle training protocol is (10 sec.
on time - 50 sec.
off time - 10 minutes total time)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain scoring
Time Frame: 6 weeks
|
pain measured by VAS tool, 0 the least pain while 10 the highest one
|
6 weeks
|
|
Quality of life by using Oswestry Disability Index (OID)
Time Frame: 6 weeks
|
questioner, Score from 0 to 19% indicate minimal disability- 20 to 39% represent moderate disability- 40 to 59% represent severe disability- 60 to 79% represent crippled disability- and scores from 80 to 100% represents patients that are confined to bed
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle thickness assessment
Time Frame: 6 weeks
|
Ultrasonography
|
6 weeks
|
|
Stability and mobility of spine
Time Frame: 6 weeks
|
Spinal mouse assessment spinal vertebrate from 7th cervical vertebrae to 3rd sacral vertebrae
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 10, 2024
Primary Completion (Actual)
June 30, 2024
Study Completion (Actual)
July 31, 2024
Study Registration Dates
First Submitted
July 2, 2024
First Submitted That Met QC Criteria
July 2, 2024
First Posted (Actual)
July 10, 2024
Study Record Updates
Last Update Posted (Actual)
June 26, 2025
Last Update Submitted That Met QC Criteria
June 24, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- physio 224
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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